NDC 69230-321 – Levocetirizine Dihydrochloride

Levocetirizine Dihydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC69230-321

Product details

Brand name
Levocetirizine Dihydrochloride
Generic name
Levocetirizine Dihydrochloride
Labeler
Camber Consumer Care Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213513
Marketed since
October 28, 2020
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Levocetirizine dihydrochloride →

Package NDC codes (6)

Package NDCDescriptionSince
69230-321-0110 BLISTER PACK in 1 CARTON (69230-321-01) / 10 TABLET, FILM COATED in 1 BLISTER PACKOct 28, 2020
69230-321-101000 TABLET, FILM COATED in 1 BOTTLE (69230-321-10)Oct 28, 2020
69230-321-311 BOTTLE in 1 CARTON (69230-321-31) / 35 TABLET, FILM COATED in 1 BOTTLEOct 28, 2020
69230-321-321 BOTTLE in 1 CARTON (69230-321-32) / 55 TABLET, FILM COATED in 1 BOTTLEOct 28, 2020
69230-321-331 BOTTLE in 1 CARTON (69230-321-33) / 80 TABLET, FILM COATED in 1 BOTTLEOct 28, 2020
69230-321-341 BOTTLE in 1 CARTON (69230-321-34) / 180 TABLET, FILM COATED in 1 BOTTLEOct 28, 2020

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